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Biological Activities of NHC-Pd(II) Complexes Based on

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dc.contributor.author Ibrahim, N
dc.contributor.author Touj, N
dc.contributor.author Koko, W
dc.contributor.author Khan, T
dc.contributor.author Ozdemir, I
dc.contributor.author Yasar, S
dc.contributor.author Hamdi, N
dc.date.accessioned 2022-10-11T13:12:57Z
dc.date.available 2022-10-11T13:12:57Z
dc.date.issued 2020
dc.identifier.uri http://hdl.handle.net/11616/75481
dc.description.abstract N-heterocyclic carbene (NHC) precursors (2a-i), their pyridine-enhanced precatalyst preparation stabilization and initiation (PEPPSI)-themed palladium N-heterocyclic carbene complexes (3a-i) and palladium N-heterocyclic triphenylphosphines complexes (4a-i) were synthesized and characterized by elemental analysis and H-1 NMR, C-13 NMR, IR, and LC-MS spectroscopic techniques. The (NHC)Pd(II) complexes 3-4 were tested against MCF7 and MDA-MB-231 cancer cells, Escherichia coli, methicillin-resistant Staphylococcus aureus (MRSA), Candida albicans microorganisms, Leishmania major promastigotes and amastigotes, Toxoplasma gondii parasites, and Vero cells in vitro. The biological assays indicated that all compounds are highly active against cancer cells, with an IC50 < 1.5 mu g mL(-1). Eight compounds proved antibacterial and antileishmanial activities, while only three compounds had strong antifungal activities against C. albicans. In our conclusion, compounds 3 (b, f, g, and h) and 4b are the most suitable drug candidates for anticancer, antimicrobial, and antiparasitical.
dc.source CATALYSTS
dc.title Biological Activities of NHC-Pd(II) Complexes Based on
dc.title Benzimidazolylidene N-heterocyclic Carbene (NHC) Ligands Bearing Aryl
dc.title Substituents


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